NDC 0832-1250 – Ramelteon

Ramelteon 8 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0832-1250

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213815
Marketed since
October 26, 2020
Listing expires
December 31, 2027
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (2)

Package NDCDescriptionSince
0832-1250-11100 TABLET, FILM COATED in 1 BOTTLE (0832-1250-11)Oct 26, 2020
0832-1250-3030 TABLET, FILM COATED in 1 BOTTLE (0832-1250-30)Oct 26, 2020

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